The Eyes of the World

Retinal Vascular Occlusions

I recall a conversation nearly a year ago where

Coquin de Chien

mentioned his optometrists were telling him about all the clots they were seeing lately. It made him realize that micro-clots hard to detect in most tissues, might be easily surveyed in Eye exams. It was a good non-invasive and inexpensive way to screen for this and finally someone did. The results are blinding to say the least. 2.19 hazard ratio.

This paper caught the attention of Elon Musk. Maybe Elons just realized he needs to hurry up on those self driving cars. Be a real bummer if the vax cult went blind and could no longer watch CNN and other brain melting COViD fear porn. If Tinnitus kicks in we’d have a large class of deaf, blind and brain fogged to care for.

2.19 hazard ratio. Notice the Nerf language is attenuated to “May not be a coincidental finding after COVID-19 vaccination”.

Congratulations! Your Nature paper tested Vaccidental Coinciditis negative.

There are many things that could be leading to the clotting from both the virus and the vaccine. The most published culprit is the protein they share; spike protein but the vaccine has a unique route of administration (IV) that presents a unique risk profile.

My favorite unsung hypothesis on this is from Marc Girardot of

Covid Myth Buster Series

where IV injection with LNPs paint the target cells for destruction by the immune system. In this hypothesis, the spike is just the tracer molecule that provides the signature of the criminal. Its toxicity, while noted, is unlikely to be the sole pathogen/toxin due to concentration. The LNPs simply need any antigen that transfects and paints cells for destruction. Your immune system then napalms any tissue painted (transfected) with LNPs.

Our spike myopia has certainly offered Marc a lot of flack for his contra-spike position but its important to note that we have no vehicle controls on these vaccines. If all blame is placed onto spike, you should get ready for LNP vaccines for RSV and every other non-spike antigen they can dream of being placed into you.

An argument for spike being the sole problem opens the door for them to torture you with a different peptides every year and I still have a lot of questions about how these other adjuvants/antigens might effectively paint the targets in future vaccines.

Let’s take a look at another contaminant in the vaccines.

We now know there is dsDNA contamination in the vaccines and we have provided evidence that this dsDNA is packaged in the LNPs and transfection ready.

Can dsDNA injections explain any of these adverse events?

Prothrombotic phenotype. Hmmm.

Please explain..

Unacceptable Jessica

has covered VAERs data prolifically and I recall a lot of thrombotic events.

This study used 5ng/ul quantities of dsDNA in cationic lipids. This is on the high side of what we see in our vax dsDNA contamination studies. Agilent and Qubit detect it in this range but those technologies might be picking up some RNA in the process. qPCR suggests a 100 fold less than this (40pg/ul) but 300 ul of this is injected in the form of LNPs. Total dose is 12ng according to the most conservative qPCR measurements.

There is important language in here that speaks to Fibrinolytic molecule tissue plasminogen activator.

So the dsDNA activates this. This is also seen in DNA vaccines and in mRNA vaccines we now know are contaminated with dsDNA.

Some of this activity also occurs with the virus so we can’t place all of the blame on the doorstep of dsDNA contamination. We can place some blame on the regulators who seem to provide a hall pass for Pharma every time one of their defects is detected. The RNA integrity loss going from the trials to the larger scale up is a prime example.

This brings us back to ‘Spike Myopia’ as an argument against these vaccines. This singular focus of pathogenicity enables pharma to swap out spike and repeat the crime claiming they’ve repented and cleaned up their sins.

I’m not so certain of this. I think we need to fundamentally rethink the broad scale/non targeted transfection with dirty products. Too much IV risk. Too many unknowns.

Late next week I will be heading to the CannMed conference down in Marco Island Florida where I am on 3 panels and giving a talk on the Hop Latent viroid pandemic spreading across the Cannabis industry. This conference is held at a kush Marriot with impeccable beaches and facilities. It’s a family friendly get away conference that is focused on alternative medicine.

Cannabinoids, Psilocybin, and any natural compound that can aid in personalized medicine. This physician base understands what it is like dealing with horse paste accusations for decades. You can learn how to build work around markets with medical legalization movements and how to take drug QC into your own hands with lab testing and analytical chemistry.

Many long COVID patients are benefiting from Cannabinoids.

John Campbell just gave a great presentation on a few papers explaining why. We have one of the authors in this space presenting on this topic. It is a much deeper rabbit hole. John is just touching the surface of the literature on cannabinoids with a focus on antiviral activity. What he is missing in this presentation is that COVID is a disease of comorbidities and cannabinoids address most of these COVID comorbidities.

Anticoagulant effects of a Cannabis extract in an obese rat model

Therapeutic Potential of Non-Psychotropic Cannabidiol in Ischemic Stroke

Effects of cannabis oil extract on immune response gene expression in human small airway epithelial cells (HSAEpC): implications for chronic obstructive pulmonary disease (COPD)

Come join us if you can.